Pontzer C H, Newton-Nash D K, Garancis J C, Abramoff P
Department of Comparative and Experimental Pathology, University of Florida, Gainesville 32610.
Reg Immunol. 1988 Sep-Oct;1(2):119-27.
Subclasses of lung immunoregulatory T cells were analyzed during acute pulmonary inflammation in strain 2 guinea pigs and compared with T cell subpopulations in the peripheral circulation. Immunized animals were aerosol-challenged with specific antigen and sacrificed at 12-, 24-, 48-, 72-, and 96-hours postchallenge. Mononuclear cells, isolated from peripheral blood and bronchoalveolar lavage, were enriched for T cells. The percentage of helper T cells, as well as antigen-specific blastogenesis, in recovered pulmonary T cells exhibited maximal values at 12-, 24-, and 96-hours postchallenge. In contrast, the presence of suppressor T cells correlated with decreased blastogenesis and antigen-specific suppression in isolated lung cells at 72-hours postchallenge. Since changes in pulmonary cells did not correlate with those found in the peripheral circulation, immunoregulatory events in these two compartments may be distinct. These results indicate that the proportions of lung T cell subclasses, as well as their in vitro functional activity, are altered over the course of pulmonary disease. Such changes in immunoregulatory cell populations may be important in the mediation of disease pathogenesis.
在2型豚鼠急性肺部炎症期间,分析了肺部免疫调节性T细胞的亚类,并与外周循环中的T细胞亚群进行了比较。对免疫动物进行特定抗原的气溶胶攻击,并在攻击后12、24、48、72和96小时处死。从外周血和支气管肺泡灌洗中分离出的单核细胞经富集得到T细胞。回收的肺部T细胞中辅助性T细胞的百分比以及抗原特异性增殖反应在攻击后12、24和96小时呈现最大值。相比之下,在攻击后72小时,抑制性T细胞的存在与分离的肺细胞中增殖反应降低和抗原特异性抑制相关。由于肺部细胞的变化与外周循环中发现的变化不相关,这两个区室中的免疫调节事件可能是不同的。这些结果表明,肺部T细胞亚类的比例及其体外功能活性在肺部疾病过程中会发生改变。免疫调节细胞群体的这种变化可能在疾病发病机制的介导中起重要作用。